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慢性髓性白血病患者的淋巴增殖性疾病:一项单中心病例系列研究

Lymphoproliferative Disorders in Patients with Chronic Myeloid Leukemia: A Single-Center Case Series.

作者信息

Alshehry Nawal F, Al-Huneini Mohammed, Lipton Jeffrey H, Michelis Fotios V

机构信息

Department of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, Ont., Canada.

出版信息

Acta Haematol. 2015;134(3):161-7. doi: 10.1159/000375150. Epub 2015 May 9.

DOI:10.1159/000375150
PMID:25968918
Abstract

Lymphoproliferative disorders presenting simultaneously with or subsequent to the occurrence of chronic myeloid leukemia (CML) have rarely been reported. Herein, we report 8 cases of a variety of lymphoproliferative conditions associated with CML at different times during the course of the disease. All 8 patients were treated with tyrosine kinase inhibitors at some point during the course of their illness. The literature regarding the uncommon association of these apparently unrelated disorders is reviewed as well as the possible underlying mechanisms that could be associated with this phenomenon.

摘要

同时出现或在慢性髓性白血病(CML)发生后出现的淋巴增殖性疾病鲜有报道。在此,我们报告8例在疾病过程中不同时间与CML相关的各种淋巴增殖性疾病。所有8例患者在病程中的某个时间点均接受了酪氨酸激酶抑制剂治疗。本文回顾了关于这些明显无关疾病罕见关联的文献,以及可能与此现象相关的潜在机制。

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Lymphoproliferative Disorders in Patients with Chronic Myeloid Leukemia: A Single-Center Case Series.慢性髓性白血病患者的淋巴增殖性疾病:一项单中心病例系列研究
Acta Haematol. 2015;134(3):161-7. doi: 10.1159/000375150. Epub 2015 May 9.
2
[Bcr-Abl inhibition as molecular therapy approach in chronic myeloid leukemia].[作为慢性髓性白血病分子治疗方法的Bcr-Abl抑制作用]
Med Klin (Munich). 2002 Jan 15;97 Suppl 1:2-6.
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BCR-ABL kinase domain mutations in tyrosine kinase inhibitors-naïve and -exposed Southeast Asian chronic myeloid leukemia patients.未接受过酪氨酸激酶抑制剂治疗和已暴露于酪氨酸激酶抑制剂的东南亚慢性髓性白血病患者的 BCR-ABL 激酶结构域突变。
Exp Mol Pathol. 2012 Apr;92(2):259-65. doi: 10.1016/j.yexmp.2012.01.007. Epub 2012 Jan 31.
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Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the Philadelphia chromosome.BCR-ABL酪氨酸激酶特异性抑制剂在伴有费城染色体的慢性髓性白血病急变期和急性淋巴细胞白血病中的活性
N Engl J Med. 2001 Apr 5;344(14):1038-42. doi: 10.1056/NEJM200104053441402.
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Case report and literature review: a rare patient with chronic myeloid leukemia and chronic lymphocytic leukemia.病例报告与文献综述:一例罕见的慢性髓系白血病合并慢性淋巴细胞白血病患者。
Ann Clin Lab Sci. 2008 Autumn;38(4):405-9.
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Novel targeted therapies to overcome imatinib mesylate resistance in chronic myeloid leukemia (CML).克服慢性粒细胞白血病(CML)中甲磺酸伊马替尼耐药性的新型靶向疗法。
Crit Rev Oncol Hematol. 2006 Feb;57(2):145-64. doi: 10.1016/j.critrevonc.2005.06.007. Epub 2005 Oct 5.
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Dasatinib: a tyrosine kinase inhibitor for the treatment of chronic myelogenous leukemia and philadelphia chromosome-positive acute lymphoblastic leukemia.达沙替尼:一种用于治疗慢性粒细胞白血病和费城染色体阳性急性淋巴细胞白血病的酪氨酸激酶抑制剂。
Clin Ther. 2007 Nov;29(11):2289-308. doi: 10.1016/j.clinthera.2007.11.005.
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Ponatinib: A new tyrosine kinase inhibitor for the treatment of chronic myeloid leukemia and Philadelphia chromosome-positive acute lymphoblastic leukemia.普纳替尼:一种新型酪氨酸激酶抑制剂,用于治疗慢性髓性白血病和费城染色体阳性急性淋巴细胞白血病。
Ann Pharmacother. 2013 Nov;47(11):1540-6. doi: 10.1177/1060028013501144. Epub 2013 Nov 21.
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Detection of BCR-ABL gene mutations in Philadelphia chromosome positive leukemia patients resistant to STI-571 cancer therapy.对STI-571癌症治疗耐药的费城染色体阳性白血病患者中BCR-ABL基因突变的检测
Leuk Res. 2008 Nov;32(11):1724-34. doi: 10.1016/j.leukres.2008.04.023. Epub 2008 Jul 7.
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A limited but necessary indication of stem cell transplantation for chronic myelogeneous leukemia in the era of tyrosine kinase inhibitors.在酪氨酸激酶抑制剂时代,慢性髓性白血病干细胞移植的一种有限但必要的指征。
Transplantation. 2014 Jan 15;97(1):e4-5. doi: 10.1097/01.TP.0000437675.24458.25.

引用本文的文献

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Dasatinib-associated follicular lymphoma in a patient with B-cell acute lymphoblastic leukaemia.达沙替尼相关滤泡性淋巴瘤在 B 细胞急性淋巴细胞白血病患者中的发生。
BMJ Case Rep. 2023 May 17;16(5):e252739. doi: 10.1136/bcr-2022-252739.
2
Dasatinib associated lymphadenopathy in a chronic myeloid leukemia patient: A case report.达沙替尼相关性淋巴结病在一名慢性髓性白血病患者中的病例报告
Medicine (Baltimore). 2020 Nov 6;99(45):e22791. doi: 10.1097/MD.0000000000022791.